Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63865857-63865986 | Common:1; Rare:33 | ||||
chr21:32521413-32521716 | Common:2; Rare:56 | ||||
chr21:36430102-36430359 | Common:2; Rare:53 | ||||
chr21:39676579-39676742 | Common:1; Rare:29 | ||||
chr21:45317567-45317779 | Common:1; Rare:45 | ||||
chr21:45319578-45319844 | Common:2; Rare:64 | ||||
chr22:19176623-19176864 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
chr22:20783844-20784123 | Rare:69; Clinvar:1 | ||||
chr22:30420599-30420778 | Common:2; Rare:31 | ||||
chr22:30969036-30969278 | Common:2; Rare:69 | ||||
chr22:36288802-36289301 | Common:2; Rare:146; Clinvar:5; Clinvar (benign):8 | ||||
chr22:36331568-36331752 | Common:2; Rare:34 | ||||
chr22:38176171-38176205 | Rare:4 | ||||
chr22:46052802-46052905 | Rare:21 | ||||
chr22:46069860-46070067 | Rare:46 |